铂金
锗
催化作用
密度泛函理论
离解(化学)
兴奋剂
质谱法
材料科学
选择性
化学
计算化学
化学工程
纳米技术
无机化学
物理化学
硅
有机化学
光电子学
色谱法
工程类
作者
Andoni Ugartemendia,Kristien Peeters,Piero Ferrari,Abel de Cózar,José M. Mercero,Ewald Janssens,Elisa Jimenez‐Izal
出处
期刊:ChemPhysChem
[Wiley]
日期:2021-05-31
卷期号:22 (15): 1603-1610
被引量:10
标识
DOI:10.1002/cphc.202100407
摘要
The vulnerability towards CO poisoning is a major drawback affecting the efficiency and long-term performance of platinum catalysts in fuel cells. In the present work, by a combination of density functional theory calculations and mass spectrometry experiments, we test and explain the promotional effect of Ge on Pt catalysts with higher resistance to deactivation via CO poisoning. A thorough exploration of the configurational space of gas-phase Ptn + and GePtn-1 + (n=5-9) clusters using global minima search techniques and the subsequent electronic structure analysis reveals that germanium doping reduces the binding strength between Pt and CO by hindering the 2π-back-donation. Importantly, the clusters remain catalytically active towards H2 dissociation. The ability of Ge to weaken the Pt-CO interaction was confirmed by mass spectrometry experiments. Ge can be a promising alloying agent to tune the selectivity and improve the durability of Pt particles, thus opening the way to novel catalytic alternatives for fuel cells.
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